Results 161 to 170 of about 1,727,695 (209)

Toward a better definition of EPCAM deletions in Lynch Syndrome: Report of new variants in Italy and the associated molecular phenotype. [PDF]

Mol Genet Genomic Med, 2019
Cini G, Quaia M, Canzonieri V, Fornasarig M, Maestro R, Morabito A, D'Elia AV, Urso ED, Mammi I, Viel A.   +9 more
europepmc   +1 more source

Effect of felzartamab anti-CD38 treatment on the molecular phenotype of antibody-mediated rejection in kidney transplant biopsies.

Halloran P, Diebold M, Gauthier P, Mayer K, Mackova M, Hinze C, Chang J, Patel U, Schütz E, Schrezenmeier E, Budde K, Böhmig G.   +11 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Molecular Phenotyping for Severe Asthma

Personalized Medicine, 2008
Evaluation of: Brasier AR, Sundar V, Boetticher G et al.: Molecular phenotyping of severe asthma using pattern recognition of bronchoalveolar lavage-derived cytokines. J. Allergy Clin. Immunol. 121, 30-37 (2008). Asthma is a heterogeneous disorder presenting with many phenotypes.
Patricia, Noel, Weiniu, Gan, James, Kiley   +2 more
openaire   +2 more sources

Molecular Determinants of Temperature-Sensitive Phenotypes

Biochemistry, 2019
Temperature-sensitive (Ts) mutants are important tools for understanding the role of essential gene(s), but their molecular basis is not well understood. We use CcdB ( Controller of Cell Death protein B) as a model system to explore the effects of Ts mutations on protein stability, folding, and ligand binding.
Arti Tripathi, Shiv Swaroop, Raghavan Varadarajan   +2 more
openaire   +2 more sources

MOLECULAR BASIS OF OBESITY PHENOTYPES

Pediatria. Journal named after G.N. Speransky, 2021
The review summarizes data on the molecular mechanisms of interaction between different components of adipose tissue under physiological conditions and in obesity. Body mass (BM) index is the most popular, but not the only indicator of metabolism. In practical medicine, four phenotypes need to be operated on: metabolically unhealthy and healthy obesity
N.N. Smirnova, N.B. Kuprienko, V.P. Novikova, E.V. Zudinova   +3 more
openaire   +1 more source

Molecular Basis of Weak D Phenotypes

Blood, 1999
A Rhesus D (RhD) red blood cell phenotype with a weak expression of the D antigen occurs in 0.2% to 1% of whites and is called weak D, formerly Du. Red blood cells of weak D phenotype have a much reduced number of presumably complete D antigens that were repeatedly reported to carry the amino acid sequence of the regular RhD protein.
F F, Wagner, C, Gassner, T H, Müller, D, Schönitzer, F, Schunter, W A, Flegel   +5 more
openaire   +2 more sources

Craniosynostoses: Phenotypic/molecular correlations

American Journal of Medical Genetics, 1995
From the discovery of the first known human homeobox mutation in MSX2 for craniosynostosis of the Boston type by Jams to the recent report of 2 mutations in FGFR2 in Apert syndrome by Wilkie, it is clear that the molecular aspects of syndromes with craniosynostosis are becoming known at a dizzying pace. Four of the syndromes involve mutations in FGFR2.
openaire   +2 more sources

Synovial Tissue: Cellular and Molecular Phenotyping

Current Rheumatology Reports, 2019
This review provides a summary of recent molecular findings that have refined our understanding of the cell types that constitute human synovial tissue, particularly in patients with rheumatoid arthritis (RA).Recent advances in high-dimensional and single-cell assays have elucidated upwards of 20 cell subsets in the RA synovium.
Sara, Shanaj, Laura T, Donlin
openaire   +2 more sources